Extraordinary People Season 2
Extraordinary People is a television documentary series broadcast on Channel 5 in the United Kingdom. Each programme follows the lives of people with a rare medical condition or unusual ability. People featured have or had rare illnesses such as rabies and eye cancer. Many of these people do activities previously thought impossible for people in their condition. The show began airing on 28 March 2003.
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Extraordinary People
2003Extraordinary People is a television documentary series broadcast on Channel 5 in the United Kingdom. Each programme follows the lives of people with a rare medical condition or unusual ability. People featured have or had rare illnesses such as rabies and eye cancer. Many of these people do activities previously thought impossible for people in their condition. The show began airing on 28 March 2003.
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Extraordinary People Season 2 Full Episode Guide
In this episode of Extraordinary People, a group of people suffer from a rare condition called Dystonia. Dystonia is a neurological muscle disorder that causes uncontrollable, painful spasms anywhere in the body. Although not very well known, it is estimated that there are more than 500,000 people in North America alone that have the disease. This is more than Muscular Dystrophy, Huntington's Disease, and Lou Gehrig's disease combined.
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Novemthree, five years old, was born on November 3, in Indonesia. When he was three, tumors started growing in his face. They became so large, his face was distorted and he could hardly breathe or eat. A radical surgery was his only hope.
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This is the story of three young men who suffer from Tourette's Syndrome. Some of the symptoms of this disorder are involuntary muscle twitching, tics, and even loud verbal outbursts.
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Helen has a multiple personality disorder, probably caused by childhood abuse. Helen's lifelong friend, Dr. Ruth Selwyn, investigates the different personalities, ranging from childish to suicidal.
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Archie is just two years old and weighs almost six stone, or 84 pounds. He has a rare genetic disease called MOMO syndrome, which belongs to the family of overgrowth syndromes. This disease has only been diagnosed in four cases in the world. The name is an acronym of the four primary aspects of the disorder: Macrosomia (excessive birth weight), Obesity, Macrocephaly (excessive head size) and Ocular abnormalities.
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